Carlos Cervera

738 total citations
20 papers, 465 citations indexed

About

Carlos Cervera is a scholar working on Molecular Biology, Rheumatology and Neurology. According to data from OpenAlex, Carlos Cervera has authored 20 papers receiving a total of 465 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 9 papers in Rheumatology and 6 papers in Neurology. Recurrent topics in Carlos Cervera's work include Glycogen Storage Diseases and Myoclonus (9 papers), Mitochondrial Function and Pathology (4 papers) and Neurogenetic and Muscular Disorders Research (4 papers). Carlos Cervera is often cited by papers focused on Glycogen Storage Diseases and Myoclonus (9 papers), Mitochondrial Function and Pathology (4 papers) and Neurogenetic and Muscular Disorders Research (4 papers). Carlos Cervera collaborates with scholars based in Spain, United States and Palestinian Territory. Carlos Cervera's co-authors include Josep Gámez, Antoni L. Andreu, Montserrat Baiget, Carmen Navarro, José M. Fernández, Eduardo F. Tizzano, Michio Hirano, Ivon Cuscó, M. J. Barceló and Guillermo Izquierdo and has published in prestigious journals such as Neurology, Annals of Neurology and American Journal of Ophthalmology.

In The Last Decade

Carlos Cervera

20 papers receiving 447 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Carlos Cervera Spain 13 291 156 143 89 86 20 465
Pascal Laforêt France 9 178 0.6× 118 0.8× 85 0.6× 41 0.5× 36 0.4× 18 367
Roula Ghaoui Australia 10 300 1.0× 25 0.2× 121 0.8× 83 0.9× 131 1.5× 22 486
Adrian G. Todd United States 12 276 0.9× 60 0.4× 157 1.1× 54 0.6× 50 0.6× 20 449
Astrid Brull Spain 13 216 0.7× 198 1.3× 17 0.1× 83 0.9× 66 0.8× 22 398
Edgard Verdura Spain 8 255 0.9× 31 0.2× 45 0.3× 122 1.4× 57 0.7× 17 389
Francesco Laschena Italy 12 419 1.4× 25 0.2× 104 0.7× 41 0.5× 172 2.0× 18 534
Manu Jokela Finland 12 236 0.8× 18 0.1× 119 0.8× 114 1.3× 83 1.0× 35 356
M.P. Freda Italy 10 559 1.9× 17 0.1× 87 0.6× 17 0.2× 157 1.8× 11 616
Stefan‐M. Pulst United States 11 346 1.2× 37 0.2× 27 0.2× 270 3.0× 298 3.5× 19 566
Ichiro Imafuku Japan 11 224 0.8× 30 0.2× 54 0.4× 117 1.3× 128 1.5× 30 458

Countries citing papers authored by Carlos Cervera

Since Specialization
Citations

This map shows the geographic impact of Carlos Cervera's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Carlos Cervera with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Carlos Cervera more than expected).

Fields of papers citing papers by Carlos Cervera

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Carlos Cervera. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Carlos Cervera. The network helps show where Carlos Cervera may publish in the future.

Co-authorship network of co-authors of Carlos Cervera

This figure shows the co-authorship network connecting the top 25 collaborators of Carlos Cervera. A scholar is included among the top collaborators of Carlos Cervera based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Carlos Cervera. Carlos Cervera is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Cuscó, Ivon, M. J. Barceló, Ricard Rojas‐García, et al.. (2005). SMN2 copy number predicts acute or chronic spinal muscular atrophy but does not account for intrafamilial variability in siblings. Journal of Neurology. 253(1). 21–25. 86 indexed citations
2.
Gámez, Josep, Fermín Mearin, N. Raguer, et al.. (2004). A novel thymidine phosphorylase mutation in a Spanish MNGIE patient. Journal of the Neurological Sciences. 228(1). 35–39. 15 indexed citations
3.
Nogales‐Gadea, Gisela, Elena García‐Arumí, Antoni L. Andreu, Carlos Cervera, & Josep Gámez. (2003). A novel exon 5 mutation (N139H) in the SOD1 gene in a Spanish family associated with incomplete penetrance. Journal of the Neurological Sciences. 219(1-2). 1–6. 18 indexed citations
4.
Palenzuela, Lluís, Antoni L. Andreu, Josep Gámez, et al.. (2003). A novel autosomal dominant limb-girdle muscular dystrophy (LGMD 1F) maps to 7q32.1-32.2. Neurology. 61(3). 404–406. 37 indexed citations
5.
Segovia‐Silvestre, Toni, Antoni L. Andreu, Cristòfol Vives-Bauzá, et al.. (2002). A novel exon 3 mutation (D76V) in the SOD1 gene associated with slowly progressive ALS. Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders. 3(2). 69–74. 18 indexed citations
6.
Gámez, Josep, M. J. Barceló, Xavier Muñoz, et al.. (2002). Survival and respiratory decline are not related to homozygous SMN2 deletions in ALS patients. Neurology. 59(9). 1456–1460. 22 indexed citations
7.
Gámez, Josep, Luisa Guarner, S. Tadesse, et al.. (2002). Phenotypic variability in a Spanish family with MNGIE. Neurology. 59(3). 455–457. 35 indexed citations
8.
Campos, Yolanda, Josep Gámez, Antoni L. Andreu, et al.. (2001). A new mtDNA mutation in the tRNALeu(UUR) gene associated with ocular myopathy. Neuromuscular Disorders. 11(5). 477–480. 12 indexed citations
9.
Gámez, Josep, Carmen Navarro, Antoni L. Andreu, et al.. (2001). Autosomal dominant limb-girdle muscular dystrophy. Neurology. 56(4). 450–454. 38 indexed citations
10.
Gámez, Josep, et al.. (2001). Bilateral optic nerve atrophy in myotonic dystrophy. American Journal of Ophthalmology. 131(3). 398–400. 2 indexed citations
11.
Martı́n, Miguel A., Carlos Rubio-Terrés, Pilar del Hoyo, et al.. (2001). Molecular heterogeneity of myophosphorylase deficiency (Mcardle's disease): A genotype-phenotype correlation study. Annals of Neurology. 50(5). 574–574. 3 indexed citations
12.
Martı́n, Miguel A., Carlos Rubio-Terrés, Pilar del Hoyo, et al.. (2001). Molecular heterogeneity of myophosphorylase deficiency (Mcardle's disease): A genotype‐phenotype correlation study. Annals of Neurology. 50(5). 574–581. 79 indexed citations
13.
Gámez, Josep, Adriana Lasa, E. del Rı́o, et al.. (1999). Novel mutations in the muscle chloride channel CLCN1 gene causing myotonia congenita in Spanish families. Journal of Neurology. 246(9). 825–829. 18 indexed citations
14.
Fernández, Roberto, José M. Fernández, Carlos Cervera, et al.. (1999). Adult glycogenosis II with paracrystalline mitochondrial inclusions and Hirano bodies in skeletal muscle. Neuromuscular Disorders. 9(3). 136–143. 23 indexed citations
15.
Andreu, Antoni L., Claudio Bruno, Josep Gámez, et al.. (1999). A new mutation in the myophosphorylase gene (Asn684Tyr) in a Spanish patient with McArdle's disease. Neuromuscular Disorders. 9(3). 171–173. 15 indexed citations
16.
Gámez, Josep, Roberto Fernández, Claudio Bruno, et al.. (1999). A new mutation in the regulatory domain of the myophosphorylase gene affecting protein dimer contact. Muscle & Nerve. 22(8). 1136–1138. 11 indexed citations
17.
Gámez, Josep, Roberto Fernández, Claudio Bruno, et al.. (1999). A new mutation in the regulatory domain of the myophosphorylase gene affecting protein dimer contact. Muscle & Nerve. 22(8). 1136–1138. 3 indexed citations
18.
Andreu, Antoni L., Claudio Bruno, Josep Gámez, et al.. (1998). Molecular genetic analysis of McArdle's disease in Spanish patients. Neurology. 51(1). 260–262. 23 indexed citations
19.
Fernández, José M., Josep Gámez, Carlos Cervera, et al.. (1997). Distal myopathy of Miyoshi and Nonaka types: a clinical, pathological and quantitative EMG study of 7 cases. Neuromuscular Disorders. 7(6-7). 462–463. 1 indexed citations
20.
Sancho, Sara, Carmen Navarro, José M. Fernández, et al.. (1990). Skin biopsy findings in glycogenosis III: Clinical, biochemical, and electrophysiological correlations. Annals of Neurology. 27(5). 480–486. 6 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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